Canonical Allele Identifier: CA413594459

Gene: PHKA1

Linked Data

• gnomAD v4: X-72667398-C-T
• MyVariant Identifiers: chrX:g.71887248C>T (hg19) ; chrX:g.72667398C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.72667398C>T , CM000685.2:g.72667398C>T	GRCh38
NC_000023.10:g.71887248C>T , CM000685.1:g.71887248C>T	GRCh37
NC_000023.9:g.71803973C>T	NCBI36
NG_016599.1:g.51782G>A
NG_016599.2:g.51784G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373542.9:c.694G>A MANE Select	ENSP00000362643.4:p.Ala232Thr
ENST00000339490.7:c.694G>A	ENSP00000342469.3:p.Ala232Thr
ENST00000373539.3:c.694G>A	ENSP00000362640.3:p.Ala232Thr
ENST00000373542.8:c.694G>A	ENSP00000362643.4:p.Ala232Thr
ENST00000373545.7:c.694G>A	ENSP00000362646.3:p.Ala232Thr
ENST00000541944.5:c.694G>A	ENSP00000441251.1:p.Ala232Thr
NM_001122670.1:c.694G>A	NP_001116142.1:p.Ala232Thr
NM_001172436.1:c.694G>A	NP_001165907.1:p.Ala232Thr
NM_002637.3:c.694G>A	NP_002628.2:p.Ala232Thr
XM_006724661.2:c.694G>A	XP_006724724.1:p.Ala232Thr
XR_001755696.1:n.837G>A
NM_002637.4:c.694G>A MANE Select	NP_002628.2:p.Ala232Thr
NM_001122670.2:c.694G>A	NP_001116142.1:p.Ala232Thr
NM_001172436.2:c.694G>A	NP_001165907.1:p.Ala232Thr